Non-coding RNA may be associated with cytoplasmic male sterility in Silene vulgaris

被引:25
作者
Stone, James D. [1 ,2 ]
Kolouskova, Pavla [1 ]
Sloan, Daniel B. [3 ]
Storchova, Helena [1 ]
机构
[1] Acad Sci Czech Republ, Inst Expt Bot, Vvi, Rozvojova 263, CR-16502 Prague, Czech Republic
[2] Acad Sci Czech Republ, Inst Bot, Vvi, Pruhonice 25243, Central Bohemia, Czech Republic
[3] Colorado State Univ, Dept Biol, Ft Collins, CO 80523 USA
基金
美国国家科学基金会;
关键词
Cytoplasmic male sterility; editing; mitochondrion; non-coding RNA; Silene vulgaris; splicing; transcriptome; MASSIVE MITOCHONDRIAL GENOME; OPEN READING FRAME; MESSENGER-RNAS; EDITING SITES; SEQ DATA; GENES; ANGIOSPERM; TRANSCRIPTOME; NUCLEAR; COMPLEX;
D O I
10.1093/jxb/erx057
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Cytoplasmic male sterility (CMS) is a widespread phenomenon in flowering plants caused by mitochondrial (mt) genes. CMS genes typically encode novel proteins that interfere with mt functions and can be silenced by nuclear fertility-restorer genes. Although the molecular basis of CMS is well established in a number of crop systems, our understanding of it in natural populations is far more limited. To identify CMS genes in a gynodioecious plant, Silene vulgaris, we constructed mt transcriptomes and compared transcript levels and RNA editing patterns in floral bud tissue from female and hermaphrodite full siblings. The transcriptomes from female and hermaphrodite individuals were very similar overall with respect to variation in levels of transcript abundance across the genome, the extent of RNA editing, and the order in which RNA editing and intron splicing events occurred. We found only a single genomic region that was highly overexpressed and differentially edited in females relative to hermaphrodites. This region is not located near any other transcribed elements and lacks an open-reading frame (ORF) of even moderate size. To our knowledge, this transcript would represent the first non-coding mt RNA associated with CMS in plants and is, therefore, an important target for future functional validation studies.
引用
收藏
页码:1599 / 1612
页数:14
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